I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Trouillard, Oriane
110
results:
Search for persons
X
Format
Online (110)
Mediatypes
Articles (Online) (28)
OpenAccess-fulltext (82)
Sorted by: Relevance
Sorted by: Year
?
1
Comment on "Defining the Genetic Landscape of Congenital Mi..:
Trouillard, Oriane
;
Méneret, Aurélie
;
Dunoyer, Margaux
...
Movement Disorders. 39 (2024) 5 - p. 925-926 , 2024
Link:
https://doi.org/10.1002/..
?
2
Rare Missense Variants in KCNJ10 Are Associated with Paroxy..:
Wirth, Thomas
;
Roze, Emmanuel
;
Delvallée, Clarisse
...
Movement Disorders. 39 (2024) 5 - p. 897-905 , 2024
Link:
https://doi.org/10.1002/..
?
3
Mirror Movements Due To a TUBB3 Variant:
Desjardins, Clément
;
Gras, Domitille
;
Trouillard, Oriane
...
Pediatric Neurology. 148 (2023) - p. 142-144 , 2023
Link:
https://doi.org/10.1016/..
?
4
SCN1A-related epilepsy with recessive inheritance: Two furt..:
Moretti, Raffaella
;
Arnaud, Lionel
;
Bouteiller, Delphine
...
European Journal of Paediatric Neurology. 33 (2021) - p. 121-124 , 2021
Link:
https://doi.org/10.1016/..
?
5
The supplementary motor area modulates interhemispheric int..:
Welniarz, Quentin
;
Gallea, Cécile
;
Lamy, Jean‐Charles
...
Human Brain Mapping. 40 (2019) 7 - p. 2125-2142 , 2019
Link:
https://doi.org/10.1002/..
?
6
Association of Rare Genetic Variants in Opioid Receptors wi..:
Depienne, Christel
;
Ciura, Sorana
;
Trouillard, Oriane
...
Tremor and Other Hyperkinetic Movements. 9 (2019) 0 - p. , 2019
Link:
https://doi.org/10.5334/..
?
7
Cover Image, Volume 39, Issue 1:
Marsh, Ashley P. L.
;
Edwards, Timothy J.
;
Galea, Charles
...
Human Mutation. 39 (2017) 1 - p. i-i , 2017
Link:
https://doi.org/10.1002/..
?
8
Non cell-autonomous role of DCC in the guidance of the cort..:
Welniarz, Quentin
;
Morel, Marie-Pierre
;
Pourchet, Oriane
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
9
DCCmutation update: Congenital mirror movements, isolated a..:
Marsh, Ashley P. L.
;
Edwards, Timothy J.
;
Galea, Charles
...
Human Mutation. 39 (2017) 1 - p. 23-39 , 2017
Link:
https://doi.org/10.1002/..
?
10
Congenital Mirror Movements Due to RAD51: Cosegregation wit..:
Trouillard, Oriane
;
Koht, Jeanette
;
Gerstner, Thorsten
...
Tremor and Other Hyperkinetic Movements. 6 (2016) 0 - p. 424 , 2016
Link:
https://doi.org/10.5334/..
?
11
ADCY5-related dyskinesia: Broader spectrum and genotype–phe..:
Chen, Dong-Hui
;
Méneret, Aurélie
;
Friedman, Jennifer R.
...
Neurology. 85 (2015) 23 - p. 2026-2035 , 2015
Link:
https://doi.org/10.1212/..
?
12
ADCY5 mutation carriers display pleiotropic paroxysmal day ..:
Friedman, Jennifer R.
;
Méneret, Aurélie
;
Chen, Dong‐Hui
...
Movement Disorders. 31 (2015) 1 - p. 147-148 , 2015
Link:
https://doi.org/10.1002/..
?
13
Congenital mirror movements: From piano player to opera sin..:
Méneret, Aurélie
;
Welniarz, Quentin
;
Trouillard, Oriane
.
Neurology. 84 (2015) 8 - p. 860-860 , 2015
Link:
https://doi.org/10.1212/..
?
14
Congenital mirror movements caused by a mutation in theDCCg..:
Meneret, Aurelie
;
Trouillard, Oriane
;
Brochard, Vanessa
.
Developmental Medicine & Child Neurology. 57 (2015) 8 - p. 776-776 , 2015
Link:
https://doi.org/10.1111/..
?
15
Congenital mirror movements: no mutation in DNAL4 in 17 ind..:
Méneret, Aurélie
;
Trouillard, Oriane
;
Vidailhet, Marie
..
Journal of Neurology. 261 (2014) 10 - p. 2030-2031 , 2014
Link:
https://doi.org/10.1007/..
1-15